US5955455AExpiredUtility

Therapeutic methods and delivery systems utilizing sex steroid precursors

87
Assignee: ENDORECHERCHE INCPriority: Jan 19, 1993Filed: Nov 13, 1997Granted: Sep 21, 1999
Est. expiryJan 19, 2013(expired)· nominal 20-yr term from priority
Inventors:Fernand Labrie
A61P 5/26A61P 5/00A61P 9/00A61P 5/34A61P 3/10A61P 9/10A61P 25/00A61P 3/04A61P 25/28A61P 35/00A61P 15/02A61P 13/00A61K 31/58C07J 43/006A61P 19/04C07J 1/0011A61P 15/00A61K 8/63A61K 31/57A61K 31/565A61P 15/12A61Q 19/00C07J 43/003A61P 17/00A61P 19/10A61P 21/00A61P 15/18A61K 31/566A61K 31/5685A61P 19/00
87
PatentIndex Score
47
Cited by
41
References
6
Claims

Abstract

Sex steroid precursors such as dehydroepiandrosterone and dehydroepiandrosterone sulphate, and compounds converted in vivo to either of the foregoing, are utilized for the treatment of vaginal atrophy, hypogonadism, diminished libido, loss of collagen or connective tissues in the skin, and, in combination with an estrogen and/or progestin, for the treatment of menopause. The precursors may be formulated for percutaneous or transmucosal administration. Gels, solutions, lotions, creams, ointments and transdermal patches for the administration of these precursors are provided, as are certain pharmaceutical compositions and kits which can be used for the prevention and treatment of a wide variety of conditions related to decreased secretion of sex steroid precursors by the adrenals.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
       1. A pharmaceutical composition in the form of a transdermal or percutaneous cream, ointment, or lotion, said pharmaceutical composition comprising a carrier having dissolved therein at least one sex steroid precursor selected from the group consisting of dehydroepiandrosterone, dehydroepiandrosterone sulphate, and compounds converted in vivo to either of the foregoing, said precursor being present at a concentration of at least 7% by weight relative to the total pharmaceutical composition suitable for achieving and maintaining a serum level concentration 4 to 13 micrograms per liter, and said carrier being compatible with skin or mucosa and allowing penetration of said precursor through said skin or mucosa, said carrier having sufficient viscosity to maintain said precursor on a localized area of skin or mucosa, without running or evaporating, for a time period sufficient to permit substantial penetration of said precursor through said localized area of said skin or mucosa. 
     
     
       2. The pharmaceutical composition of claim 1 wherein said carrier includes a mixture of a pharmaceutically acceptable solvent and at least one thickening agent. 
     
     
       3. The pharmaceutical composition of claim 2 wherein said carrier includes a mixture of organic and inorganic solvents. 
     
     
       4. The pharmaceutical composition of claim 3 wherein said carrier includes water and alcohol. 
     
     
       5. The pharmaceutical composition of claim 4 wherein said precursor is DHEA. 
     
     
       6. The pharmaceutical composition of claim 4 wherein said precursor is DHEA-S.

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